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HRID 279132作成日:2026年10月27日

Acetone → 2-Isopropylsulfonyl-3-(3-methoxyphenylamino)-3-methylsulfanyl-2-propenenitrile

https://huagongshe.com/reaction/279132

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物3-Methoxyphenyl isothiocyanateHCID 137832—
反応物2-(Propane-1-sulfonyl)acetonitrileHCID 519441—
生成物2-Isopropylsulfonyl-3-(3-methoxyphenylamino)-3-methylsulfanyl-2-propenenitrileHCID 7014957999%

反応手順

A solution of 2-propanesulfonylacetonitrile (2.0 g, 13.6 mmol) in dry acetone (25 ml) was stirred while dry potassium carbonate (1.28 g, 9.28 mmol) and 3-methoxyphenyl isothiocyanate (2.36 g, 14.3 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 20 h. Excess of potassium carbonate was filtered off, methyl iodide (2.54 ml, 40.8 mmol) was added to the filtrate, and stirring was continued for 60 h. The mixture was evaporated and the residue was dissolved in dichloromethane and extracted with water and brine. The organic phase was dried over magnesium sulphate, filtered and evaporated to afford 4.40 g (99%) of the title compound as yellow crystals. Mp 107-110° C. 1H NMR (200 MHz, CDCl3): δ=1.44 (d, 6H), 2.22 (s, 3H), 3.36 (heptet, 1H), 3.83 (s, 3H), 6.81 (m, 1H), 6.85 (dd, 1H), 6.87 (dd, 1H), 7.32 (dd, 1H), 9.91 (br s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362205B1
出典データセットuspto-grants-2002_03
ORD IDord-2c7e2b5e9ea945faa2c9111ef17e37ca
出典メモuspto-grants-2002_03